A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073254



Internal ID21462489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131454738..131454738hg38UCSC Ensembl
chr11:131324632..131324632hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661095
Supporting Variants
SamplesHG03009
Known GenesNTM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073254
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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